Transfergurt XL mit Clip / Transfer sling XL with clips (UDI 04260713250185)
Manufactured by BEKA-Hospitec GmbH
Device Regulatory Overview
The Transfergurt XL mit Clip / Transfer sling XL with clips (Model/Catalog Number: K119 BEKA Gurte – Lifter Zubehöre) is a medical device manufactured by BEKA-Hospitec GmbH. This product is indexed under FDA Product Code / Category Classification V0805038002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K119 BEKA Gurte – Lifter Zubehöre
- Product Code / EMDN
- V0805038002
- Device Name
- Transfergurt XS mit Clip / Transfer sling XS with clips
- Database Sync Date
- 2026-08-09 16:28:50
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Transfergurt XL mit Clip / Transfer sling XL with clips?
The registered manufacturer of record for Transfergurt XL mit Clip / Transfer sling XL with clips is BEKA-Hospitec GmbH.
What is the Primary UDI-DI identifier for Transfergurt XL mit Clip / Transfer sling XL with clips?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260713250185.
What classification code is assigned to this device?
This device is registered under product classification code V0805038002.
Similar Classification Devices (V0805038002)
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